Berkel Caglar, Cacan Ercan
Department of Molecular Biology and Genetics, Tokat Gaziosmanpasa University, Tokat, Turkey.
Immunol Res. 2023 Feb;71(1):15-28. doi: 10.1007/s12026-022-09323-7. Epub 2022 Oct 3.
Gasdermin proteins (GSDMs) form pores in cell membranes upon various stimuli, leading to the release of certain proinflammatory molecules such as IL-1β and IL-18, and this ultimately results in pyroptotic cell death. NINJ1 (Ninjurin 1) has recently been identified as a cell membrane protein responsible for the final complete plasma membrane rupture following lytic cell death mechanisms including pyroptosis, causing the release of relatively larger molecules such as HMGB1 and LDH. In this study, we reported the presence of higher GSDMD and lower GSDME protein levels in ovarian tumors compared to surrounding non-malignant stroma in the tumor microenvironment. GSDME protein levels are also lower in the tumors of the omentum compared to adjacent stromal cells. We found that NINJ1 expression decreases from early to late stage in serous ovarian cancer, and the percentage of NINJ1 copy number loss events is the highest in ovarian cancer among other cancers. Moreover, we showed that low expression of NINJ1 is associated with shorter overall survival of patients with ovarian cancer. In support of the findings showing that low NINJ1 expression contributes to worse prognosis in this most lethal gynecological malignancy, NINJ1 expression was found to be lower in cisplatin-resistant ovarian cancer cells compared to cisplatin-sensitive counterparts in vitro. We suggest that the members of gasdermin family might have distinct functions in serous ovarian cancer, and low levels of NINJ1 might contribute, at least in part, to the progression and poorer prognosis of ovarian cancer. A complete picture of how pyroptosis and subsequent plasma membrane rupture are involved in ovarian cancer will be of high importance in order to identify actionable therapeutic vulnerabilities within this newly identified group of proteins.
Gasdermin蛋白(GSDMs)在各种刺激下会在细胞膜上形成孔道,导致某些促炎分子如IL-1β和IL-18的释放,最终导致细胞焦亡。NINJ1(Ninjurin 1)最近被鉴定为一种细胞膜蛋白,它在包括细胞焦亡在内的溶解性细胞死亡机制后负责最终的完全质膜破裂,导致相对较大的分子如HMGB1和LDH的释放。在本研究中,我们报告与肿瘤微环境中周围的非恶性基质相比,卵巢肿瘤中GSDMD蛋白水平较高而GSDME蛋白水平较低。与相邻的基质细胞相比,大网膜肿瘤中的GSDME蛋白水平也较低。我们发现,在浆液性卵巢癌中,NINJ1表达从早期到晚期逐渐降低,并且在所有癌症中,卵巢癌中NINJ1拷贝数缺失事件的百分比最高。此外,我们表明NINJ1低表达与卵巢癌患者较短的总生存期相关。为了支持低NINJ1表达导致这种最致命的妇科恶性肿瘤预后更差这一发现,在体外,与顺铂敏感的卵巢癌细胞相比,顺铂耐药的卵巢癌细胞中NINJ1表达更低。我们认为,gasdermin家族成员在浆液性卵巢癌中可能具有不同的功能,NINJ1水平较低可能至少部分导致卵巢癌的进展和较差的预后。为了在这一新鉴定的蛋白质组中确定可操作的治疗靶点,全面了解细胞焦亡及随后的质膜破裂如何参与卵巢癌将非常重要。